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Becton Dickinson & Company

Becton Dickinson & Company Recalls

All product recalls associated with Becton Dickinson & Company.

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Recall Summary

Total Recalls

1000

Past Year

1000

Class I (Serious)

Most Recent

Jan 2026

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 20081–20100 of 21319 recalls

Becton Dickinson & Company: BD Syringes - #309585 -- Piston Syringe, Syringe 3ML LL...

The firm believes that some of the syringes in the affected lots may not have received the intended sterilization dose.

FDAMay 25, 2005Nationwide• Becton Dickinson & Company

Becton Dickinson & Company: # 309603 -- Syringe 5Ml LL syringe.

The firm believes that some of the syringes in the affected lots may not have received the intended sterilization dose.

FDAMay 25, 2005Nationwide• Becton Dickinson & Company

Siemens Medical Solutions USA, Inc: Mammomat Novation Digital Mammography System. Model numbe...

potential issue (image acquisition may become interrupted) when using multiple network nodes

FDAMay 25, 2005

1...1003 100410051006 1007...1066

Page 1005 of 1066Next

Nationwide

• Siemens Medical Solutions USA, Inc

Becton Dickinson & Company: #309644 -- 10 ml syringe with 20 G1'' Needle

The firm believes that some of the syringes in the affected lots may not have received the intended sterilization dose.

FDAMay 25, 2005Nationwide• Becton Dickinson & Company

Becton Dickinson & Company: # 309604 -- Syringe 10 mL LL

The firm believes that some of the syringes in the affected lots may not have received the intended sterilization dose.

FDAMay 25, 2005Nationwide• Becton Dickinson & Company

Becton Dickinson & Company: #309661 -- Syringe only ll 20 mL

The firm believes that some of the syringes in the affected lots may not have received the intended sterilization dose.

FDAMay 25, 2005Nationwide• Becton Dickinson & Company

B. Braun Medical, Inc.: Right Heart Catheter Product Line: Catalog Number 601129...

Reports in a small percentage of Right Heart Catheter Products Line related to cracked catheter tips, leaking at the manifold and cracked hubs.

FDAMay 25, 2005Nationwide• B. Braun Medical, Inc.

Becton Dickinson & Company: #309604 -- 10 mL syringe

The firm believes that some of the syringes in the affected lots may not have received the intended sterilization dose.

FDAMay 25, 2005Nationwide• Becton Dickinson & Company

Radiometer America Inc: Package Insert which accompanies the Hematocrit and Metab...

The package insert, which accompanied the QC reagents used with ABL blood gas analyzers, referenced incorrect control ranges for Hct (hematocrit) testing. The range stated on the package insert was too low to generate accurate Hct test results (The control ranges were acceptable for the glucose and lactate testing).

FDAMay 24, 2005Nationwide• Radiometer America Inc

Synovis Surgical Inovation Div. of: Peri-Strips Dry with Veritas Collagen Matrix Staple Line ...

Device is contained in 2 pouches. The outer pouch's seal may be compromised; this may render the exterior of the interior pouch non-sterile.

FDAMay 23, 2005AL, AK, AZ +10 more• Synovis Surgical Inovation Div. of

Toshiba American Med Sys Inc: Aplio Diagnostic Ultrasound System (SSA-700A and SSA-770A...

If the measurement mode is started from the Doppler mode and then the sweep speed setting is changed by the assigned user function, the measurement of the time direction results don't correspond to the actual values.

FDAMay 23, 2005Nationwide• Toshiba American Med Sys Inc

Provalis Diagnostics: Product is in2it A1C In-Office Analyzer Test Cartridge. ...

Provalis Diagnostics discovered, following its internal stability testing program (mid-point batch testing), that occasional low values were being found across multiple lots of in2it HbA1C Test Cartridges.

FDAMay 20, 2005AZ, FL, GA +5 more• Provalis Diagnostics

Roche Diagnostics Corp.: ACCU-CHEK Compact Care Kit; catalog number 3149137.

The meter may self-start without a sample having been applied and report erroneous results without an error message if the nose cover is not properly snapped in place and the undosed test strip is bent upwards while the meter is waiting for the sample, or if excess control solution or blood has been applied to the test strip.

FDAMay 18, 2005Nationwide• Roche Diagnostics Corp.

Roche Diagnostics Corp.: ACCU-CHEK Instant Meter; Catalog numbers 914 and 924.

The meter may self-start without a sample having been applied and report erroneous results without an error message if an undosed test strip is bent upwards while the meter is waiting for the sample or if the test strip opening has been previously flooded with excess control solution or blood.

FDAMay 18, 2005Nationwide• Roche Diagnostics Corp.

Roche Diagnostics Corp.: ACCU-CHEK Instant Care Kit; Catalog number 91490.

FDAMay 18, 2005Nationwide• Roche Diagnostics Corp.

Roche Diagnostics Corp.: ACCU-CHEK Compact Meter; catalog number 3183572.

FDAMay 18, 2005Nationwide• Roche Diagnostics Corp.

Kydex Glock Holsters (Michaels of Oregon) – Design Flaw (2005)

The recall includes Kydex Belt and Tactical Holsters with thumb break fits for Glock model handguns. The holsters are rigid and are made of black Kydex and come with tension screws for a proper fit. The words, "Uncle Mike's by Michaels of Oregon" are printed on the back of the holster. The recall involves sizes 12, 21, and 25, which is printed on the inside of the holster between the two screws securing the holster to the belt slide.

CPSCMay 17, 2005Nationwide• Michaels of Oregon, of Oregon City, Ore.

Smiths Medical ASD, Inc.: Portex Per-Fit Percutaneous Dilational Tracheostomy Kit ,...

Guiding catheter may have thinner and weaker sidewalls than designed, and may break.

FDAMay 16, 2005Nationwide• Smiths Medical ASD, Inc.

Stryker Howmedica Osteonics Corp.: The TRIO Spondylolisthesis Reduction Instrument is a Clas...

The threaded part of the instrument may break when connected to the screw and potentially result in an adverse health consequence.

FDAMay 16, 2005Nationwide• Stryker Howmedica Osteonics Corp.

Theragenics Corporation: PG910 Spacers, Part number SP101, loaded into Bard Expres...

The spacers loaded in the seeding cartridges were expired and/or the extra loose spacers were labeled with an incorrect expiration date.

FDAMay 16, 2005OH, VA• Theragenics Corporation